Cleared Traditional

SWIRL - A PRE-MOISTENED CLEANING TISSUE FOR EYES (K874681) - FDA 510(k) Clearance

Class I Ophthalmic device.

K874681 · Klockner Contract Packaging, Inc. · Ophthalmic device
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Feb 1988
Decision
84d
Days
Class 1
Risk

K874681 is an FDA 510(k) clearance for the SWIRL - A PRE-MOISTENED CLEANING TISSUE FOR EYES. Classified as Lens, Spectacle, Non-custom (prescription) (product code HQG), Class I - General Controls.

Submitted by Klockner Contract Packaging, Inc. (Richmond, US). The FDA issued a Cleared decision on February 5, 1988 after a review of 84 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.5844 - the FDA ophthalmic device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Klockner Contract Packaging, Inc. devices

Submission Details

510(k) Number K874681 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 13, 1987
Decision Date February 05, 1988
Days to Decision 84 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
26d faster than avg
Panel avg: 110d · This submission: 84d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code HQG Lens, Spectacle, Non-custom (prescription)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 886.5844
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.